Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox1 |
T |
G |
1: 58,102,665 (GRCm39) |
L527R |
probably damaging |
Het |
Ccdc172 |
T |
A |
19: 58,525,723 (GRCm39) |
C194S |
possibly damaging |
Het |
Ccnb1ip1 |
G |
T |
14: 51,031,121 (GRCm39) |
T64K |
possibly damaging |
Het |
Ces1b |
T |
C |
8: 93,806,109 (GRCm39) |
E44G |
probably benign |
Het |
Coro2a |
A |
T |
4: 46,543,421 (GRCm39) |
Y317* |
probably null |
Het |
Csnk1a1 |
T |
C |
18: 61,711,829 (GRCm39) |
F281S |
probably damaging |
Het |
Ddx28 |
A |
T |
8: 106,737,248 (GRCm39) |
|
probably null |
Het |
Dtnbp1 |
A |
G |
13: 45,084,721 (GRCm39) |
|
probably null |
Het |
Eif2s1 |
T |
C |
12: 78,930,126 (GRCm39) |
I258T |
possibly damaging |
Het |
Elp3 |
T |
C |
14: 65,784,488 (GRCm39) |
*554W |
probably null |
Het |
Golga1 |
T |
C |
2: 38,910,118 (GRCm39) |
M610V |
probably damaging |
Het |
Hc |
T |
A |
2: 34,935,906 (GRCm39) |
K156N |
probably benign |
Het |
Hcls1 |
G |
A |
16: 36,782,748 (GRCm39) |
G428D |
probably benign |
Het |
Il16 |
T |
C |
7: 83,371,677 (GRCm39) |
D43G |
probably damaging |
Het |
Klhl3 |
C |
A |
13: 58,242,930 (GRCm39) |
K91N |
probably damaging |
Het |
L3mbtl1 |
C |
T |
2: 162,790,095 (GRCm39) |
|
probably benign |
Het |
Lamc3 |
T |
C |
2: 31,810,544 (GRCm39) |
F805L |
possibly damaging |
Het |
Lipg |
T |
C |
18: 75,081,275 (GRCm39) |
M269V |
probably benign |
Het |
Ly75 |
G |
A |
2: 60,148,720 (GRCm39) |
T1203I |
probably benign |
Het |
Mat1a |
T |
A |
14: 40,827,561 (GRCm39) |
V5E |
probably benign |
Het |
Muc16 |
A |
T |
9: 18,548,866 (GRCm39) |
L5809Q |
probably benign |
Het |
Naip6 |
G |
A |
13: 100,420,266 (GRCm39) |
R1335C |
probably benign |
Het |
Ndufaf3 |
T |
C |
9: 108,443,416 (GRCm39) |
H128R |
probably benign |
Het |
Nphp4 |
A |
T |
4: 152,587,464 (GRCm39) |
|
probably null |
Het |
Or8u8 |
T |
A |
2: 86,012,309 (GRCm39) |
I49F |
probably damaging |
Het |
Otop3 |
T |
C |
11: 115,230,673 (GRCm39) |
V148A |
probably damaging |
Het |
Ovgp1 |
T |
C |
3: 105,893,747 (GRCm39) |
|
probably benign |
Het |
Pcsk5 |
T |
G |
19: 17,488,744 (GRCm39) |
R1025S |
probably benign |
Het |
Pkd1l2 |
T |
C |
8: 117,767,405 (GRCm39) |
D1295G |
probably benign |
Het |
Polr1d |
T |
A |
5: 147,015,359 (GRCm39) |
L14* |
probably null |
Het |
Rab26 |
T |
A |
17: 24,748,595 (GRCm39) |
K270* |
probably null |
Het |
Rasgef1c |
T |
A |
11: 49,862,246 (GRCm39) |
N378K |
probably damaging |
Het |
Rpl7a |
T |
C |
2: 26,801,536 (GRCm39) |
V76A |
probably benign |
Het |
Samd9l |
T |
A |
6: 3,377,229 (GRCm39) |
I11F |
possibly damaging |
Het |
Styxl1 |
C |
G |
5: 135,784,350 (GRCm39) |
G211A |
probably benign |
Het |
Taar9 |
T |
C |
10: 23,984,945 (GRCm39) |
Y163C |
probably damaging |
Het |
Tmem198 |
T |
A |
1: 75,457,017 (GRCm39) |
F48I |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,595,073 (GRCm39) |
N12032I |
probably damaging |
Het |
Ubr7 |
T |
A |
12: 102,727,723 (GRCm39) |
C82S |
probably damaging |
Het |
Wwtr1 |
T |
C |
3: 57,483,159 (GRCm39) |
E48G |
possibly damaging |
Het |
Zfp108 |
T |
C |
7: 23,960,819 (GRCm39) |
V470A |
probably damaging |
Het |
Zfp612 |
C |
A |
8: 110,816,181 (GRCm39) |
Q424K |
possibly damaging |
Het |
Zscan4-ps1 |
T |
C |
7: 10,802,761 (GRCm39) |
T13A |
probably benign |
Het |
|
Other mutations in Smarca2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01368:Smarca2
|
APN |
19 |
26,751,694 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01907:Smarca2
|
APN |
19 |
26,675,865 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02039:Smarca2
|
APN |
19 |
26,693,537 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02110:Smarca2
|
APN |
19 |
26,650,140 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02561:Smarca2
|
APN |
19 |
26,693,582 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02649:Smarca2
|
APN |
19 |
26,617,986 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02880:Smarca2
|
APN |
19 |
26,654,024 (GRCm39) |
splice site |
probably benign |
|
IGL03028:Smarca2
|
APN |
19 |
26,655,712 (GRCm39) |
splice site |
probably benign |
|
IGL03187:Smarca2
|
APN |
19 |
26,650,224 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03213:Smarca2
|
APN |
19 |
26,601,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03354:Smarca2
|
APN |
19 |
26,597,303 (GRCm39) |
missense |
probably benign |
0.01 |
Genghis
|
UTSW |
19 |
26,597,284 (GRCm39) |
missense |
possibly damaging |
0.53 |
kraft
|
UTSW |
19 |
26,655,763 (GRCm39) |
missense |
probably damaging |
0.99 |
Kublai
|
UTSW |
19 |
26,618,013 (GRCm39) |
missense |
probably damaging |
1.00 |
Samarkand
|
UTSW |
19 |
26,631,864 (GRCm39) |
nonsense |
probably null |
|
tashkent
|
UTSW |
19 |
26,698,273 (GRCm39) |
missense |
probably benign |
0.06 |
Xanadu
|
UTSW |
19 |
26,659,452 (GRCm39) |
missense |
possibly damaging |
0.52 |
FR4737:Smarca2
|
UTSW |
19 |
26,608,399 (GRCm39) |
unclassified |
probably benign |
|
PIT1430001:Smarca2
|
UTSW |
19 |
26,626,493 (GRCm39) |
missense |
probably benign |
0.35 |
R0184:Smarca2
|
UTSW |
19 |
26,669,649 (GRCm39) |
nonsense |
probably null |
|
R0306:Smarca2
|
UTSW |
19 |
26,618,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Smarca2
|
UTSW |
19 |
26,668,762 (GRCm39) |
missense |
probably damaging |
0.99 |
R0565:Smarca2
|
UTSW |
19 |
26,659,275 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0610:Smarca2
|
UTSW |
19 |
26,668,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R0669:Smarca2
|
UTSW |
19 |
26,683,600 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0726:Smarca2
|
UTSW |
19 |
26,675,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R1184:Smarca2
|
UTSW |
19 |
26,748,333 (GRCm39) |
splice site |
probably benign |
|
R1256:Smarca2
|
UTSW |
19 |
26,659,373 (GRCm39) |
missense |
probably benign |
0.06 |
R1299:Smarca2
|
UTSW |
19 |
26,749,011 (GRCm39) |
critical splice donor site |
probably null |
|
R1306:Smarca2
|
UTSW |
19 |
26,748,388 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1381:Smarca2
|
UTSW |
19 |
26,608,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R1400:Smarca2
|
UTSW |
19 |
26,654,140 (GRCm39) |
missense |
probably damaging |
0.98 |
R1415:Smarca2
|
UTSW |
19 |
26,688,084 (GRCm39) |
missense |
probably null |
0.72 |
R1496:Smarca2
|
UTSW |
19 |
26,608,501 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1582:Smarca2
|
UTSW |
19 |
26,729,305 (GRCm39) |
missense |
probably damaging |
0.99 |
R1666:Smarca2
|
UTSW |
19 |
26,624,434 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1668:Smarca2
|
UTSW |
19 |
26,624,434 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1751:Smarca2
|
UTSW |
19 |
26,617,780 (GRCm39) |
splice site |
probably benign |
|
R1861:Smarca2
|
UTSW |
19 |
26,601,284 (GRCm39) |
missense |
probably benign |
0.03 |
R1962:Smarca2
|
UTSW |
19 |
26,650,124 (GRCm39) |
nonsense |
probably null |
|
R1964:Smarca2
|
UTSW |
19 |
26,650,124 (GRCm39) |
nonsense |
probably null |
|
R1998:Smarca2
|
UTSW |
19 |
26,608,493 (GRCm39) |
missense |
probably benign |
0.33 |
R2014:Smarca2
|
UTSW |
19 |
26,661,305 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2255:Smarca2
|
UTSW |
19 |
26,748,438 (GRCm39) |
missense |
probably benign |
0.01 |
R2392:Smarca2
|
UTSW |
19 |
26,618,050 (GRCm39) |
critical splice donor site |
probably null |
|
R2439:Smarca2
|
UTSW |
19 |
26,668,854 (GRCm39) |
critical splice donor site |
probably null |
|
R3030:Smarca2
|
UTSW |
19 |
26,729,429 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3195:Smarca2
|
UTSW |
19 |
26,661,222 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3430:Smarca2
|
UTSW |
19 |
26,668,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R3710:Smarca2
|
UTSW |
19 |
26,646,290 (GRCm39) |
unclassified |
probably benign |
|
R3845:Smarca2
|
UTSW |
19 |
26,698,273 (GRCm39) |
missense |
probably benign |
0.06 |
R4013:Smarca2
|
UTSW |
19 |
26,661,327 (GRCm39) |
splice site |
probably null |
|
R4014:Smarca2
|
UTSW |
19 |
26,661,327 (GRCm39) |
splice site |
probably null |
|
R4016:Smarca2
|
UTSW |
19 |
26,661,327 (GRCm39) |
splice site |
probably null |
|
R4271:Smarca2
|
UTSW |
19 |
26,698,349 (GRCm39) |
critical splice donor site |
probably null |
|
R4471:Smarca2
|
UTSW |
19 |
26,597,277 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4612:Smarca2
|
UTSW |
19 |
26,753,625 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4730:Smarca2
|
UTSW |
19 |
26,608,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Smarca2
|
UTSW |
19 |
26,631,883 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4999:Smarca2
|
UTSW |
19 |
26,698,255 (GRCm39) |
nonsense |
probably null |
|
R5015:Smarca2
|
UTSW |
19 |
26,668,788 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5320:Smarca2
|
UTSW |
19 |
26,668,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R5393:Smarca2
|
UTSW |
19 |
26,617,829 (GRCm39) |
missense |
probably benign |
0.18 |
R5503:Smarca2
|
UTSW |
19 |
26,659,446 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5503:Smarca2
|
UTSW |
19 |
26,601,336 (GRCm39) |
missense |
probably damaging |
0.96 |
R5715:Smarca2
|
UTSW |
19 |
26,626,522 (GRCm39) |
missense |
probably benign |
0.16 |
R5790:Smarca2
|
UTSW |
19 |
26,654,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R5874:Smarca2
|
UTSW |
19 |
26,753,469 (GRCm39) |
intron |
probably benign |
|
R6209:Smarca2
|
UTSW |
19 |
26,748,404 (GRCm39) |
nonsense |
probably null |
|
R6236:Smarca2
|
UTSW |
19 |
26,673,613 (GRCm39) |
missense |
probably benign |
0.33 |
R6291:Smarca2
|
UTSW |
19 |
26,608,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6292:Smarca2
|
UTSW |
19 |
26,608,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6325:Smarca2
|
UTSW |
19 |
26,655,763 (GRCm39) |
missense |
probably damaging |
0.99 |
R6544:Smarca2
|
UTSW |
19 |
26,608,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R6572:Smarca2
|
UTSW |
19 |
26,656,573 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6589:Smarca2
|
UTSW |
19 |
26,597,284 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6804:Smarca2
|
UTSW |
19 |
26,729,286 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6922:Smarca2
|
UTSW |
19 |
26,668,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R7047:Smarca2
|
UTSW |
19 |
26,646,555 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7213:Smarca2
|
UTSW |
19 |
26,624,531 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7257:Smarca2
|
UTSW |
19 |
26,631,864 (GRCm39) |
nonsense |
probably null |
|
R7259:Smarca2
|
UTSW |
19 |
26,631,864 (GRCm39) |
nonsense |
probably null |
|
R7479:Smarca2
|
UTSW |
19 |
26,617,887 (GRCm39) |
missense |
probably benign |
0.00 |
R7512:Smarca2
|
UTSW |
19 |
26,661,209 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8158:Smarca2
|
UTSW |
19 |
26,659,448 (GRCm39) |
missense |
probably benign |
0.16 |
R8182:Smarca2
|
UTSW |
19 |
26,608,120 (GRCm39) |
missense |
probably benign |
0.39 |
R8207:Smarca2
|
UTSW |
19 |
26,654,080 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8467:Smarca2
|
UTSW |
19 |
26,597,121 (GRCm39) |
start codon destroyed |
probably null |
0.02 |
R8527:Smarca2
|
UTSW |
19 |
26,654,187 (GRCm39) |
missense |
probably damaging |
0.98 |
R8784:Smarca2
|
UTSW |
19 |
26,753,558 (GRCm39) |
missense |
probably benign |
0.17 |
R8898:Smarca2
|
UTSW |
19 |
26,608,358 (GRCm39) |
unclassified |
probably benign |
|
R9076:Smarca2
|
UTSW |
19 |
26,659,452 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9123:Smarca2
|
UTSW |
19 |
26,693,583 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9125:Smarca2
|
UTSW |
19 |
26,693,583 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9317:Smarca2
|
UTSW |
19 |
26,737,279 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9501:Smarca2
|
UTSW |
19 |
26,617,977 (GRCm39) |
missense |
probably benign |
0.04 |
R9514:Smarca2
|
UTSW |
19 |
26,659,452 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9641:Smarca2
|
UTSW |
19 |
26,656,498 (GRCm39) |
missense |
possibly damaging |
0.93 |
RF001:Smarca2
|
UTSW |
19 |
26,608,421 (GRCm39) |
unclassified |
probably benign |
|
RF001:Smarca2
|
UTSW |
19 |
26,608,386 (GRCm39) |
unclassified |
probably benign |
|
RF004:Smarca2
|
UTSW |
19 |
26,608,420 (GRCm39) |
unclassified |
probably benign |
|
RF019:Smarca2
|
UTSW |
19 |
26,608,401 (GRCm39) |
unclassified |
probably benign |
|
RF021:Smarca2
|
UTSW |
19 |
26,608,397 (GRCm39) |
unclassified |
probably benign |
|
RF024:Smarca2
|
UTSW |
19 |
26,608,420 (GRCm39) |
unclassified |
probably benign |
|
RF034:Smarca2
|
UTSW |
19 |
26,608,411 (GRCm39) |
unclassified |
probably benign |
|
RF040:Smarca2
|
UTSW |
19 |
26,608,422 (GRCm39) |
unclassified |
probably benign |
|
RF041:Smarca2
|
UTSW |
19 |
26,608,421 (GRCm39) |
unclassified |
probably benign |
|
RF047:Smarca2
|
UTSW |
19 |
26,608,405 (GRCm39) |
unclassified |
probably benign |
|
RF051:Smarca2
|
UTSW |
19 |
26,608,388 (GRCm39) |
unclassified |
probably benign |
|
X0061:Smarca2
|
UTSW |
19 |
26,698,240 (GRCm39) |
missense |
probably damaging |
0.98 |
|